Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4922
Gene name Gene Name - the full gene name approved by the HGNC.
Neurotensin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NTS
Synonyms (NCBI Gene) Gene synonyms aliases
NMN-125, NN, NT, NT/N, NTS1
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q21.31
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a common precursor for two peptides, neuromedin N and neurotensin. Neurotensin is a secreted tridecapeptide, which is widely distributed throughout the central nervous system, and may function as a neurotransmitter or a neuromodulator. I
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1196318 hsa-miR-181a CLIP-seq
MIRT1196319 hsa-miR-181b CLIP-seq
MIRT1196320 hsa-miR-181c CLIP-seq
MIRT1196321 hsa-miR-181d CLIP-seq
MIRT1196322 hsa-miR-4262 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
ATF1 Unknown 7791794
CREB1 Unknown 7791794
FOS Unknown 7791794
JUN Unknown 7791794
JUND Unknown 7791794
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005184 Function Neuropeptide hormone activity IEA
GO:0005515 Function Protein binding IPI 17620610, 32296183
GO:0005576 Component Extracellular region TAS
GO:0007165 Process Signal transduction NAS 8954810
GO:0007186 Process G protein-coupled receptor signaling pathway TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
162650 8038 ENSG00000133636
Protein
UniProt ID P30990
Protein name Neurotensin/neuromedin N [Cleaved into: Large neuromedin N (NmN-125); Neuromedin N (NN) (NmN); Neurotensin (NT); Tail peptide]
Protein function Neurotensin may play an endocrine or paracrine role in the regulation of fat metabolism. It causes contraction of smooth muscle.
PDB 2LNE , 2LNF , 2LNG , 2LYW , 2OYV , 2OYW , 3F6K , 4PO7 , 5LUZ , 6UP7 , 8VJY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07421 Pro-NT_NN 7 170 Neurotensin/neuromedin N precursor Family
Sequence
Sequence length 170
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction   Peptide ligand-binding receptors
G alpha (q) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
20659557, 23483448, 25449842, 20193696
Unknown
Disease term Disease name Evidence References Source
Mental depression Mental Depression, Depressive disorder 22754041 ClinVar
Mental Depression Mental Depression GWAS
Lewy Body Disease Lewy Body Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 33493519
Breast Neoplasms Associate 19156213, 21725197
Carcinogenesis Associate 30359740, 33543354
Carcinoma Ductal Breast Associate 19156213
Carcinoma Hepatocellular Associate 23418512
Carcinoma in Situ Stimulate 30883751
Carcinoma Non Small Cell Lung Associate 31614143
Carcinoma Pancreatic Ductal Associate 17641415
Cardiovascular Diseases Associate 27312221
Cholangiocarcinoma Associate 30359740